Evidence map›Paper›PMID 29539416›Full record

ArticleCell reports2018

Cbx4 Sumoylates Prdm16 to Regulate Adipose Tissue Thermogenesis.

Qingbo Chen, Lei Huang, Dongning Pan, Lihua J Zhu, Yong-Xu Wang

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  5. Review
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  7. Review
  8. Ubiquitination and Metabolic Disease.Advances in experimental medicine and biology · 2024
    Review
  9. CBX4 suppresses CD8Theranostics · 2024
    Article
  10. Article
  11. Androgen Receptor is a Negative Regulator of PRDM16 in Beige Adipocyte.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Qingbo ChenDepartment of Molecular, Cell and Cancer Biology and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Lei HuangDepartment of Molecular, Cell and Cancer Biology and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Dongning PanKey Laboratory of Metabolism and Molecular Medicine, Department of Biochemistry and Molecular Biology, Fudan University Shanghai Medical College, Shanghai 200032, China.
Lihua J ZhuDepartment of Molecular, Cell and Cancer Biology and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Yong-Xu WangDepartment of Molecular, Cell and Cancer Biology and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA. Electronic address: yongxu.wang@umassmed.edu.
University of Massachusetts Chan Medical School · USShanghai Medical College of Fudan University · CN

Funding

Regulation of brown fat metabolism by histone demethylationR01DK076118 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WANG, YONG-XU · 2008 to 2016
$3.1M
MicroRNAs in brown fat development and metabolismR01DK098594 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WANG, YONG-XU · 2014 to 2017
$1.5M
NIDDK NIH HHS R01 DK076118NIDDK NIH HHS R01 DK098594
6 · The paper itself

Abstract

Transcriptional co-activator Prdm16 controls brown fat development and white fat browning, but how this thermogenic function is modulated post-translationally is poorly understood. Here, we report that Cbx4, a Polycomb group protein, is a SUMO E3 ligase for Prdm16 and that Cbx4-mediated sumoylation of Prdm16 is required for thermogenic gene expression. Cbx4 expression is enriched in brown fat and is induced in adipose tissue by acute cold exposure. Sumoylation of Prdm16 at lysine 917 by Cbx4 blocks its ubiquitination-mediated degradation, thereby augmenting its stability and thermogenic function. Moreover, this sumoylation event primes Prdm16 to be further stabilized by methyltransferase Ehmt1. Heterozygous Cbx4-knockout mice develop metabolic phenotypes resembling those of Prdm16-knockout mice. Furthermore, fat-specific Cbx4 knockdown and overexpression produce remarkable, opposite effects on white fat remodeling. Our results identify a modifying enzyme for Prdm16, and they demonstrate a central role of Cbx4 in the control of Prdm16 stability and white fat browning.

Indexed as

Adipocytes, BrownAnimalsCells, CulturedDNA-Binding ProteinsFemaleHEK293 CellsHumansLigasesMaleMiceMice, KnockoutPolycomb-Group ProteinsPolycomb Repressive Complex 1ProtaminesSumoylationThermogenesisCBX4 protein, humanCbx4 protein, mouseDNA-Binding ProteinsLigasesPolycomb-Group ProteinsPolycomb Repressive Complex 1Prdm16 protein, mouseprotamine 2ProtaminesTranscription Factorsbeige adipocytesbrown fatCbx4Ehmt1Prdm16SUMO E3 ligasesumoylationthermogenesisubiquitinationwhite fat browning

Identifiers

PMID29539416
PMCPMC5877417
OpenAlexW2790329626

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.